Expanding suture anchor having an actuator pin

ABSTRACT

A method and apparatus for reattaching soft tissue to a boney structure using an expanding suture anchor. The method can include providing a suture anchor and forming a cavity in the boney structure for receipt of the suture anchor. The method can also include coupling the soft tissue to a suture and coupling the suture to the suture anchor. The method can further include deploying the suture anchor to fix the suture to the suture anchor and the suture anchor to the cavity.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a divisional of U.S. patent application Ser. No. 11/451,250 filed on Jun. 12, 2006, which is a continuation-in-part of U.S. patent application Ser. No. 11/006,398 filed on Dec. 7, 2005, now U.S. Pat. No. 7,976,565 issued on Jul. 12, 2011. The disclosure of the above application is incorporated herein by reference.

FIELD

The present disclosure relates generally to suture anchors, and particularly to a method and apparatus for an expanding suture anchor having an actuator pin.

BACKGROUND

The statements in this section merely provide background information related to the present disclosure and may not constitute prior art.

Various procedures may be performed to repair soft tissue in the body. Generally, it is known to fix the soft tissue to a selected area on the bone by providing a suture through a selected portion of the soft tissue while securing the other end of the suture to the selected area on the bone using a suture anchor.

Suture anchors may be retained in the selected area of the bone via a feature of the suture anchor. In hard bone, however, the suture anchor may not fully engage the bone because the surgeon is not able to apply sufficient force to the suture. Thus, the suture may become loose in the boney structure, which could lead to increased healing times or improper healing. In addition, some of the techniques used to lock the suture to the suture anchor can be labor intensive. Therefore, it may be desirable to provide a method and apparatus for an expanding suture anchor, and a method and apparatus for locking a suture to such a suture anchor.

SUMMARY

A method for attaching a soft tissue to a boney structure. The method can include providing a suture anchor and forming a cavity in the boney structure for receipt of the suture anchor. The method can also include coupling the soft tissue to a suture and coupling the suture to the suture anchor. The method can further include deploying the suture anchor to fix the suture to the suture anchor and the suture anchor to the cavity.

Also provided is a method for attaching a soft tissue to a boney structure. The method can include providing a suture anchor defining an aperture and forming a cavity in the boney structure for receipt of the suture anchor. The method can further include coupling the soft tissue to a suture and threading at least one end of the suture through the aperture of the suture anchor. The method can include disposing the suture anchor in the cavity and deploying the suture anchor to fix the suture anchor to the cavity. The deployment of the suture anchor can fix the suture to the suture anchor without the use of a knot.

A method for attaching a soft tissue to a boney structure is also provided. The method can include providing a suture anchor and forming a cavity in the boney structure for receipt of the suture anchor. The method can also include coupling the soft tissue to a suture and coupling the suture to the suture anchor. The method can also include disposing the suture anchor in the cavity and applying a retractive force to the suture anchor. The retractive force can fix the suture in the suture anchor.

A suture anchor for attaching soft tissue to a pre-selected area of a boney structure is further provided. The suture anchor can include an expanding anchor for engaging the boney structure and an insert slideably coupled to the expanding anchor. The insert can be moveable to cause the expanding anchor to expand and engage the boney structure. An aperture can be defined in the insert, and a suture can be received in the aperture. The suture can be adapted to be coupled to the soft tissue. The movement of the insert can fix the suture to the expanding anchor.

Further areas of applicability will become apparent from the description provided herein. It should be understood that the description and specific examples are intended for purposes of illustration only and are not intended to limit the scope of the present disclosure.

DRAWINGS

The drawings described herein are for illustration purposes only and are not intended to limit the scope of the present disclosure in any way.

FIG. 1 is a perspective view of an expanding suture anchor having an actuator pin according to the present disclosure;

FIG. 2 is an exploded view of the suture anchor in FIG. 1;

FIG. 3 is a cross-sectional view taken along line 3-3 of FIG. 1;

FIG. 3A is a detailed view of FIG. 3;

FIG. 4A is an environmental view of a use of the suture anchor shown in FIG. 1;

FIG. 4B is an environmental view of the suture anchor as the retractive force is applied to move the suture anchor into the fully expanded position;

FIG. 4C is an environmental view illustrating the suture anchor in a fully expanded position;

FIG. 4D is an environmental view illustrating an alternate actuator gun for use with the suture anchor shown in FIG. 1;

FIG. 5A is an environmental view illustrating an alternate use of the suture anchor of FIG. 1 after the application of a first retractive force;

FIG. 5B is an environmental view of the suture anchor as a second retractive force is applied;

FIG. 6A is an alternate environmental view of a use of the suture anchor of FIG. 1;

FIG. 6B is an environmental view of the suture anchor of FIG. 6A during the application of a retractive force;

FIG. 7 is a perspective view of a first alternative expanding suture anchor having an actuator pin according to the present disclosure;

FIG. 8 is an environmental view of a first procedure associated with the suture anchor shown in FIG. 7;

FIG. 9 is an environmental view of a second procedure associated with the suture anchor shown in FIG. 7;

FIG. 10 is an environmental view of the suture anchor of FIG. 7 as the retractive force is applied to move the suture anchor into the fully expanded position;

FIG. 11 is an environmental view illustrating the suture anchor of FIG. 7 in a fully expanded position;

FIG. 11A is an alternative environmental partial view illustrating the suture anchor of FIG. 7 in a fully expanded position;

FIG. 12 is detailed front view of the suture anchor of FIG. 7 illustrating a suture fixed to the suture anchor;

FIG. 13 is a perspective view of a second alternative expanding suture anchor having an actuator pin according to the present disclosure;

FIG. 14 is an environmental view of a first procedure associated with the suture anchor shown in FIG. 13;

FIG. 15 is an environmental view of a second procedure associated with the suture anchor shown in FIG. 13;

FIG. 16 is detailed front view of the suture anchor of FIG. 13 illustrating a suture fixed to the suture anchor;

FIG. 17 is a perspective view of a third alternative expanding suture anchor having an actuator pin according to the present disclosure;

FIG. 18 is detailed front view of the suture anchor of FIG. 17 illustrating a suture fixed to the suture anchor;

FIG. 19 is a perspective view of a fourth alternative expanding suture anchor having an actuator pin according to the present disclosure;

FIG. 20 is detailed front view of the suture anchor of FIG. 19 illustrating a suture fixed to the suture anchor;

FIG. 21 is a perspective view of a fifth alternative expanding suture anchor having an actuator pin according to the present disclosure;

FIG. 22 is a cross-sectional view taken along line 22-22 of FIG. 21;

FIG. 23 is an environmental view of a first procedure associated with the suture anchor shown in FIG. 21;

FIG. 24 is an environmental view of a second procedure associated with the suture anchor shown in FIG. 21;

FIG. 25 is an environmental view of the suture anchor of FIG. 21 as the retractive force is applied to move the suture anchor into the fully expanded position;

FIG. 26 is an environmental view illustrating the suture anchor of FIG. 21 in a fully expanded position;

FIG. 27 is detailed front view of the suture anchor of FIG. 21 illustrating a suture fixed to the suture anchor;

FIG. 28 is a perspective view of a sixth alternative expanding suture anchor having an actuator pin according to the present disclosure;

FIG. 29 is an environmental view of a first procedure associated with the suture anchor shown in FIG. 28;

FIG. 30 is an environmental view of a second procedure associated with the suture anchor shown in FIG. 28;

FIG. 31 is detailed front view of the suture anchor of FIG. 28 illustrating a suture fixed to the suture anchor;

FIG. 32 is a perspective view of a seventh alternative expanding suture anchor having an actuator pin according to the present disclosure;

FIG. 33 is detailed front view of the suture anchor of FIG. 32 illustrating a suture fixed to the suture anchor;

FIG. 34 is a perspective view of a eighth alternative expanding suture anchor having an actuator pin according to the present disclosure;

FIG. 35 is detailed front view of the suture anchor of FIG. 34 illustrating a suture fixed to the suture anchor;

FIG. 36 is a perspective view of a ninth alternative expanding suture anchor having an actuator pin according to the present disclosure;

FIG. 36A is another perspective view of a ninth alternative expanding suture anchor having an actuator pin according to the present disclosure;

FIG. 37 is detailed front view of the suture anchor of FIG. 36 illustrating a suture fixed to the suture anchor;

FIG. 37B is another detailed front view of the suture anchor of FIG. 36 illustrating a suture fixed to the suture anchor;

FIG. 38 is a perspective view of a tenth alternative expanding suture anchor having an actuator pin according to the present disclosure;

FIG. 39 is detailed front view of the suture anchor of FIG. 38 illustrating a suture fixed to the suture anchor;

FIG. 40 is a perspective view of a eleventh alternative expanding suture anchor having an actuator pin according to the present disclosure;

FIG. 41 is an environmental view of a procedure associated with the suture anchor shown in FIG. 40; and

FIG. 42 is detailed front view of the suture anchor of FIG. 40 illustrating a suture fixed to the suture anchor.

DETAILED DESCRIPTION

The following description of various embodiments is merely exemplary in nature and is in no way intended to limit the present teachings, their application, or uses. Although the following description is related generally to a suture anchor that can be positioned in a pre-drilled hole, that is a hole provided in a boney structure for acceptance of the suture anchor, it will be understood that a suture anchor including an impacting tip or self-drilling thread may be provided as well. Moreover, it will be understood that the suture anchor, as described and claimed herein, can be used with any appropriate surgical procedure. Therefore, it will be understood that the following discussions is not intended to limit the scope of the appended claims.

With reference to FIG. 1, an expanding suture anchor 10 having an actuator pin 12 is illustrated. The suture anchor 10 is operable in a first configuration for insertion into a pre-drilled hole 14 in a boney structure 16 (as shown in FIG. 4A) and operable in a second configuration to secure the suture anchor 10 in the pre-drilled hole 14 (as shown in FIG. 4C). The suture anchor 10 generally includes an insert 18 molded to the actuator pin 12 and partially disposed in a sleeve 20.

With continuing reference to FIG. 1 and additional reference to FIGS. 2 and 3, the insert 18 includes a suture receiving portion 22 and an end section 24 displaced from the suture receiving portion 22 by a breakaway section 26. The suture receiving portion 22 and end section 24 have a tensile and a torsion strength that are greater than the tensile and torsion strength of the breakaway section 26 such that the suture receiving portion 22 and end section 24 will be severed by the breakaway section 26 without damage to the structural integrity of either section. The insert 18 is generally insert molded from a resorbable material (such as, for example, Lactosorb®, available from Biomet Inc. of Warsaw, Ind.); however, it will be understood that other types of biocompatible materials and other methods of forming could be used.

At least one groove 28 extends throughout a length L1 of the suture receiving portion 22 and the end section 24 for receipt of strands from a suture 30 therein. The suture receiving portion 22 further has a tip 32 and a cylindrical body 34. The tip 32 is generally conical in shape; however, any other desired shape may be used. The cylindrical body 34 has a diameter D1, which is sized to ensure a slip fit with the sleeve 20 such that the cylindrical body 34 can slide within the sleeve 20. The cylindrical body 34 includes a formed eyelet 36 extending through the cylindrical body 34 to provide an attachment point for the suture 30, as shown in FIG. 3A. The diameter D1 of the cylindrical body can provide an interference fit with regard to the suture 30 fitting between the cylindrical body 34 and the sleeve 20. Referring back to FIG. 3, the cylindrical body 34 may further include a tapered section 40 leading to the breakaway section 26.

The breakaway section 26 has a diameter D2, which is generally one-half the size of the diameter D1 of the cylindrical body 34. The breakaway section 26 may include two necked portions 42, 44, which facilitate the fracturing of the breakaway section 26 by reducing the fracture strength of the breakaway section 26 in torsion and tension as compared to the suture receiving portion 22 and the end section 24. The diameter of the necked portions 42, 44 may vary to enable different fracture loads for various applications; however, generally the force required to fracture the necked portions 42, 44 will be between 10-12 foot-pounds. The fracturing of the breakaway section 26 detaches the suture receiving portion 22 from the end section 24 of the insert 18 (as illustrated in FIG. 4C).

With continued reference to FIG. 3 and additional reference to FIG. 2, the end section 24 has a tapered portion 46 coupled to an annular body 48. The tapered portion 46 includes a first diameter D3 at a first end 50, which tapers to a second diameter D4 at a second end 52. In general, the first diameter D3 of the tapered portion 46 is approximately equal to the diameter D1 of the suture receiving portion 22. The tapered portion 46 operates to place the suture anchor 10 in the second position to engage the boney structure 16 as will be described in greater detail below. The second end 52 of the tapered portion 46 is coupled to the annular body 48. The annular body 48 is generally cylindrical and has a constant diameter D5. The diameter D5 of the annular body 48 may be larger than or equal to the second diameter D4 of the tapered portion 46, yet smaller than the first diameter D3 of the tapered portion 46. The annular body 48 can extend beyond the sleeve 20 when the suture anchor 10 is assembled to provide a locator 54 for an actuator gun 56 (as shown in FIG. 4A) for the application of a retractive force F1; however, this is not necessary, as will be discussed further below. The annular body 48 and tapered portion 46 each further include a formed central bore 58 for receipt of the actuator pin 12 therein.

The actuator pin 12 is fixedly attached to the annular body 48 and tapered portion 46 via insert molding. In particular, the insert 18 is formed around the actuator pin 12, ensuring secure and precise attachment. The actuator pin 12 is positioned in the formed central bore 58 of the annular body 48 and tapered portion 46 such that the actuator pin 12 is removed from the suture anchor 10 when the breakaway section 26 is fractured. The actuator pin 12 can be made of any suitable biocompatible corrosive resistance material such as, for example, surgical steel. In this regard, the actuator pin 12 need not be made of the same material as the sleeve 20.

The actuator pin 12 further includes a formed cavity 60 that retains the actuator pin 12 in the insert 18 through out the application of the retractive force F1. More specifically, as best shown in FIG. 3, as the insert 18 is formed around the actuator pin 12, material M is formed under the cavity 60. Thus, this material M must be displaced in order to remove the actuator pin 12 from the insert 18. Accordingly, the retractive force F1 must be less than the fracture strength of the material M to ensure the actuator pin 12 is retained in the insert 18. Similarly, the size of the cavity 60 can be modified to allow the accumulation of varying amounts of material M depending on the amount of retractive force F1 required to secure the suture anchor 10 in a given boney structure.

With continuing reference to FIGS. 2 and 3 and additional reference to FIG. 1, the sleeve 20 is disposed about a substantial portion of the insert 18. More specifically, the sleeve 20 includes a throughbore 62 for receipt of the insert 18 therein. The sleeve 20 has a length L, which may be configured such that the suture receiving portion 22 and locator 54 are exposed when the suture anchor 10 is in the first position. For example, a first end 64 of sleeve 20 is shown covering the breakaway section 26 and approximately one half of the cylindrical body 34 of the suture receiving portion 22 and a second end 66 of the sleeve 20 covers the tapered portion 46 and approximately one half of the annular body 48 of the end section 24. The sleeve 20 is typically made from a resorbable material (such as, for example, Lactosorb®, available from Biomet Inc. of Warsaw, Ind.); however, other suitable materials could be employed.

The sleeve 20 is generally cylindrical in nature, and may include at least one ring or securement device 68 on an external surface 70 of the sleeve 20. Although the sleeve 20 is shown having a ring 68, it is to be understood various other external features could be disposed on the sleeve 20 (such as, for example, barbs or threads). The at least one ring 68 further aids in the engagement of the suture anchor 10 in the pre-drilled hole 14. The sleeve 20 also includes at least one expanding member 72 hingably coupled to the sleeve 20 to engage the pre-drilled hole 14. Specifically, the expanding member 72 is defined by a slot 74 formed in the sleeve 20 and includes a hinge 76. In one embodiment, the sleeve 20 includes two expanding members 72 located approximately 180 degrees apart. It shall be noted, however, that the expanding members 72 could be located at any position on the sleeve 20 that would engage the boney structure 16. The expanding members 72 are located at a midsection 78 of the sleeve 20. The expanding members 72 expand to lock into the boney structure 16 when the retractive force F1 is applied to the actuator pin 12 and, in turn, to a tapered interior bearing surface 80 on the expanding members 72.

With reference now to FIG. 4A, after the pre-drilled hole 14 has been drilled into the boney structure 16 and the eyelet 36 of the insert 18 has been threaded with the suture 30, the suture anchor 10 can be inserted into the pre-drilled hole 14 as shown. The suture anchor 10 is generally configured such that only the locator 54 of the end section 24 extends beyond a top surface 82 of the boney structure 16.

Next, the actuator gun 56 is applied to the suture anchor 10 as shown in FIGS. 4A and 4B. When a trigger 84 on the actuator gun 56 is pulled, the actuator gun 56 applies the retractive force F1 to the actuator pin 12. It should be noted, however, that the actuator gun 56 may not be the only actuating device capable of applying the retractive force F1 to the suture anchor 10. In particular, numerous other devices may be employed (such as, for example, a syringe-type actuator 88, as shown in FIG. 4D). In FIG. 4D, the syringe-type actuator 88 includes a cannula 90 that engages the actuator pin 12. A lever 92 can be used to retract the cannula 90 by the application of a force F to the lever 92. More specifically, the lever 92 operates to retract the cannula 90 once it is engaged with the actuator pin 12 to provide the retractive force F1 to the suture anchor 10. A stop 94 can also be provided to prevent the lever 92 from prematurely applying the retractive force F1.

The application of the retractive force F1 causes the insert 18 to displace rearwardly with respect to the sleeve 20, as illustrated in FIG. 4B. This rearward displacement causes the tapered portion 46 to apply a force F3 to the tapered interior bearing surface 80 of the expanding members 72 of the sleeve 20. As the insert 18 continues to move rearward, the tapered portion 46 applies an increasingly greater force F3 to the tapered interior bearing surface 80 of the expanding members 72 until the expanding members 72 are engaged with the boney structure 16.

In a soft boney structure 16, when the expanding members 72 are fully engaged, the tip 32 of the suture receiving portion 22 is pressed against the first end 64 of the sleeve 20, and thus the insert 18 is not able to further retract. Hence, the continued application of the retractive force F1 causes the breakaway section 26 to fracture, as shown in FIG. 4C. With reference now to FIG. 5A, in a hard boney structure 16′, however, the breakaway section 26 may fracture prior to the tip 32 of the suture receiving portion 22 contacting the first end 64 of the sleeve 20. In this situation, the suture 30 can be pulled by a hand 86 of an operator, as illustrated in FIG. 5B, such that the tip 32 of the suture receiving portion 22 abuts the first end 64 of the sleeve 20. The pulling of the suture 30 by the hand 86 of the operator causes the expanding members 72 to expand further due to the force applied to the tapered interior bearing surface 80 of the expanding members 72 by the cylindrical body 34 of the suture receiving portion 22. In either hard or soft boney structures 16, 16′ once the breakaway section 26 fractures, the sleeve 20 and suture receiving portion 22 remain in the pre-drilled hole 14 to couple a selected soft tissue to the boney structures 16, 16′ via the suture 30.

In addition, the suture anchor 10 is also adaptable for use in a curved pre-drilled hole 14′, as shown in FIG. 6A. In this exemplary embodiment, the suture anchor 10 may be positioned in the curved pre-drilled hole 14′ via the actuator pin 12. Next, as shown in FIG. 6B, the retractive force F1 may be applied to the actuator pin 12 by an actuating device, such as the actuator gun 56, to cause the expanding members 72 to engage the boney structure 16′″, as discussed previously.

With reference to FIG. 7, a first alternative insert 18 a is shown. The first alternative insert 18 a can include a suture receiving portion 22 a, the breakaway section 26 and the end section 24 for use with a suture anchor 10 a substantially similar to that described with regard to FIGS. 1-6B. As will be appreciated, the remainder of the suture anchor 10 a can be generally similar to the suture anchor 10 that is illustrated in and described in conjunction with FIGS. 1-6B. In addition, as the breakaway section 26 and end section 24 of the first alternative insert 18 a are substantially similar to the breakaway section 26 and end section 24 of the insert 18 of the suture anchor 10, the breakaway section 26 and end section 24 will not be discussed in detail with regard to the first alternative insert 18 a. Further, the same reference numerals will be used to denote the same or similar components.

The suture receiving portion 22 a and end section 24 can have a tensile and a torsion strength that are greater than the tensile and torsion strength of the breakaway section 26 such that the suture receiving portion 22 a and end section 24 will be severed by the breakaway section 26 without damage to the structural integrity of either section. The first alternative insert 18 a is generally insert molded from a resorbable material (such as, for example, Lactosorb® available from Biomet Inc. of Warsaw, Ind.); however, it will be understood that other types of biocompatible materials and other methods of forming could be used.

As shown in FIG. 7, the suture receiving portion 22 a can include the tip 32, a cylindrical body 34 a, and a suture 30 a. The tip 32 can be generally conical in shape; however, any other desired shape may be used, such as rectangular. The cylindrical body 34 a can have a diameter D1 a, which is sized to ensure a slip fit with the sleeve 20 such that the cylindrical body 34 a can slide within the sleeve 20. The cylindrical body 34 a can define an aperture, which can be an eyelet 36 a, extending through the cylindrical body 34 a to provide an attachment point for the suture 30 a. The diameter D1 a of the cylindrical body 34 a can also provide an interference fit between the cylindrical body 34 a, the suture 30 a and the sleeve 20. The cylindrical body 34 a can further include the tapered section 40 leading to the breakaway section 26. The suture 30 a can have a first end 200, a midsection 201 and a second end 202. The eyelet 36 a can be sized to receive both the first end 200 and the second end 202 of the suture 30 a. The suture 30 a can be fixed to the cylindrical body 34 a without the use of a knot by the sleeve 20, as will be discussed herein. The midsection 201 of the suture 30 a can be coupled to a section of soft tissue 204, as shown in FIG. 8. The midsection 201 of the suture 30 a can be coupled to the soft tissue 204 through any appropriate technique, such as a mattress stitch 206 or by using a suture punch (not shown).

In order to employ the suture anchor 10 a, with the pre-drilled hole 14 drilled into the boney structure 16, the suture 30 a can be coupled to the soft tissue 204. Then, the hand 86 of the operator can thread or insert the first end 200 and the second end 202 of the suture 30 a through the eyelet 36 a. With additional reference to FIG. 9, once the first end 200 and the second end 202 of the suture 30 a are threaded through the eyelet 36 a, the suture anchor 10 a can be inserted into the pre-drilled hole 14. Generally, the first end 200 and the second end 202 of the suture 30 a can extend beyond the pre-drilled hole 14 to enable the hand 86 of the operator to grasp either or both the first end 200 and the second end 202. The hand 86 of the operator can be used to tighten the suture 30 a, and thus the soft tissue 204, to the pre-drilled hole 14 by pulling the first end 200 and second end 202 of the suture 30 a that extends from the pre-drilled hole 14. This further removes any slack from the suture 30 a. After the suture 30 a is tightened, the expanding members 72 of the suture anchor 10 a can be expanded to engage the pre-drilled hole 14.

For example, in order to expand the expanding members 72, an alternative syringe-type actuator 88′ can be coupled to the actuator pin 12 of the suture anchor 10 a as shown in FIGS. 9 and 10. The alternative syringe-type actuator 88′ can include a cannula 90′ that engages the actuator pin 12. A lever 92′ can be used to retract the cannula 90′ by the application of a force F to the lever 92′. Generally, the lever 92′ can operate to retract the cannula 90′ once it is engaged with the actuator pin 12 to provide the retractive force F1 to the suture anchor 10 a. A safety or stop 94′ can also be provided to prevent the operator from prematurely applying the retractive force F1.

In order to deploy the suture anchor 10 a in the pre-drilled hole 14, the stop 94′ can be pushed in and then the force F can be applied to the lever 92′ on the syringe-type actuator 88′, as shown in FIG. 10. When the lever 92′ on the alternative syringe-type actuator 88′ is pulled, the alternative syringe-type actuator 88′ can apply the retractive force F1 to the actuator pin 12 via the cannula 90′. It should be noted, however, that the alternative syringe-type actuator 88′ is not the only actuating device capable of applying the retractive force F1 to the suture anchor 10 a. Numerous other devices can be employed, such as, a syringe-type actuator 88, as discussed with regard to FIG. 4D, or the actuator gun 56 discussed with regard to FIGS. 4A and 4B.

The application of the retractive force F1 can cause the first alternative insert 18 a to be displaced or moved rearwardly with respect to the sleeve 20, as illustrated in FIG. 10. This rearward movement can cause the tapered portion 46 of the first alternative insert 18 a to apply a force F3 to the tapered interior bearing surface 80 of the expanding members 72 of the sleeve 20. The first alternative insert 18 a can continue to move rearward, which can cause the tapered portion 46 to apply an increasingly greater force F3 to the tapered interior bearing surface 80 of the expanding members 72 until the expanding members 72 are engaged with the boney structure 16.

When the expanding members 72 are fully engaged, the tip 32 of the suture receiving portion 22 a can be adjacent to the suture 30 a, while the suture 30 a is adjacent to the first end 64 of the sleeve 20 (as best shown in FIG. 12). The compression of the suture 30 a between the suture receiving portion 22 a and the tip 32 can fix or lock the suture 30 a to the suture anchor 10 a, while preventing the first alternative insert 18 a from retracting further. The continued application of the retractive force F1 to the first alternative insert 18 a can cause the breakaway section 26 to fracture, as shown in FIG. 11.

It should be noted, as shown in FIG. 11A, the pre-drilled hole 14 can be sized with a depth D substantially equivalent to a length L of the suture anchor 10 a, if desired. If the pre-drilled hole 14 has the depth D substantially equivalent to the length L of the suture anchor 10 a, then the expanding members 72 can be deployed or expanded by the contact of the tip 32 of the suture receiving portion 22 a against a bottom 213 of the pre-drilled hole 14. Generally, as the suture anchor 10 a is inserted, the tip 32 can be pushed against the bottom 213 of the pre-drilled hole 14, forcing the first alternative insert 18 a to be displaced or moved rearwardly with respect to the sleeve 20. This rearward movement can cause the tapered portion 46 of the first alternative insert 18 a to apply a force F3 to the tapered interior bearing surface 80 of the expanding members 72 of the sleeve 20. Then, the lever 92′ on the syringe-type actuator 88′ can be pulled (with the stop 94′ pushed in) to apply the retractive force F1 to the actuator pin 12 to fully engage the expanding members 72 in the pre-drilled hole 14. The continued application of the retractive force F1 to the first alternative insert 18 a can cause the breakaway section 26 to fracture, as shown in FIG. 11.

Once the breakaway section 26 fractures, as shown in either FIG. 11 or 11A, the sleeve 20 and suture receiving portion 22 a remain in the pre-drilled hole 14 to couple the soft tissue 204 to the boney structure 16 via the suture 30 a. The first end 200 and second end 202 of the suture 30 a that extends from the pre-drilled hole 14 can then be trimmed if desired (not shown).

As shown in FIG. 12, the suture anchor 10 a can fix the suture 30 a to the suture anchor 10 a without the use of a knot. Generally, as the first end 200 and second end 202 of the suture 30 a extend from the eyelet 36 a of the first alternative insert 18 a prior to the deployment of the expanding members 72 of the sleeve 20, the application of the retractive force F1 causes the first alternative insert 18 a, and thus suture 30 a, to be withdrawn into the sleeve 20. Thus, the movement of the first alternative insert 18 a within the sleeve 20 can fix or lock the suture 30 a to the suture anchor 10 a due to the interference fit between the first alternative insert 18 a, the suture 30 a and the sleeve 20. Further, the interference fit between the first alternative insert 18 a, the suture 30 a and the sleeve 20 can prevent the first alternative insert 18 a from moving after the deployment of the expanding members 72 due to the frictional lock created between the suture 30 a, the first alternative insert 18 a and the sleeve 20.

With reference to FIG. 13, a second alternative insert 18 b is shown. The second alternative insert 18 b can include a suture receiving portion 22 b, the breakaway section 26, and the end section 24 for use with a suture anchor 10 b substantially similar to that described with regard to FIGS. 7-12. As the breakaway section 26 and end section 24 of the second alternative insert 18 b are substantially similar to the breakaway section 26 and end section 24 of the insert 18, the breakaway section 26 and end section 24 will not be discussed in detail with regard to the second alternative insert 18 b. In addition, as the suture receiving portion 22 b is substantially similar to the suture receiving portion 22 a of the first alternative insert 18 a, as discussed with FIGS. 7-12, only the modifications to the suture receiving portion 22 b will be discussed herein.

As shown in FIG. 13, the suture receiving portion 22 b can include an aperture, for example, a groove or slot 250, which can be for receipt of the suture 30 a. Generally, the slot 250 can be formed longitudinally in a cylindrical body 34 b of the second alternative insert 18 b; however, the slot 250 can be formed in any desired position, such as vertically or diagonally. As will be appreciated, the remainder of the cylindrical body 34 b can be generally similar to the cylindrical body 34 a that is illustrated in and described in conjunction with FIG. 7.

The slot 250 can extend for a length L and can have a height H configured to enable an operator to insert the first end 200 and second end 202 of the suture 30 a through the slot 250, as shown in FIG. 14. Generally, once the midsection 201 of the suture 30 a is coupled to the soft tissue 204 via the mattress stitch 206 or any other technique, such as a suture punch (not shown), the hand 86 of the operator can thread or insert the first end 200 and second end 202 of the suture 30 a into the slot 250. Then, with reference to FIG. 15, the suture anchor 10 b can be inserted into the pre-drilled hole 14. As discussed previously, the hand 86 of the operator can be used to tighten the suture 30 a, and thus the soft tissue 204, to the pre-drilled hole 14 by pulling the first end 200 and second end 202 of the suture 30 a that extends from the pre-drilled hole 14. After the suture 30 a is tightened, the suture anchor 10 b can be deployed to engage the pre-drilled hole 14 through the use of the actuator gun 56, syringe-type actuator 88 or syringe-type actuator 88′, for example, as discussed previously with reference to FIGS. 4A and 4B, 4D and 9-12, respectively.

When the suture anchor 10 b is fully engaged to the pre-drilled hole 14, the tip 32 of the suture receiving portion 22 b can be adjacent to the suture 30 a, while the suture 30 a is adjacent to the first end 64 of the sleeve 20 (as best shown in FIG. 16). The compression of the suture 30 a between the suture receiving portion 22 b and the tip 32 can fix or lock the suture 30 a to the suture anchor 10 b. Thus, the suture anchor 10 b can also fix the suture 30 a to the suture anchor 10 b without the use of a knot, while providing greater access for the hand 86 of the operator to couple the first end 200 and the second end 202 to the second alternative insert 18 b prior to the placement of the suture anchor 10 b into the pre-drilled hole 14. The first end 200 and second end 202 of the suture 30 a that extends from the pre-drilled hole 14 can then be trimmed if desired (not shown).

With reference to FIG. 17, a third alternative insert 18 c is shown. The third alternative insert 18 c can include a suture receiving portion 22 c, the breakaway section 26, and the end section 24 for use with a suture anchor 10 c substantially similar to that described with regard to FIGS. 7-12. As the breakaway section 26 and end section 24 of the third alternative insert 18 c are substantially similar to the breakaway section 26 and end section 24 of the insert 18, the breakaway section 26 and end section 24 will not be discussed in detail with regard to the third alternative insert 18 c. In addition, as the suture receiving portion 22 c is substantially similar to the suture receiving portion 22 a of the first alternative insert 18 a, as discussed with FIGS. 7-12, only the modifications to the suture receiving portion 22 c will be discussed herein.

As shown in FIG. 17, the suture receiving portion 22 c can include a slot, for example, a C-shaped slot 260, which can be for receipt of the suture 30 a. Generally, the slot 260 can be defined in a cylindrical body 34 c of the third alternative insert 18 c. As will be appreciated, the remainder of the cylindrical body 34 c can be generally similar to the cylindrical body 34 a that is illustrated in and described in conjunction with FIG. 7. The slot 260 can define a throughbore 262 and a necked portion 264 as shown in FIGS. 17 and 18. The necked portion 264 can define an aperture 266 for receipt of the first end 200 and second end 202 of the suture 30 a. Generally, the necked portion 264 can be configured such that the first end 200 and second end 202 of the suture 30 a can be hooked behind and retained by the necked portion 264.

As the assembly and deployment of the suture anchor 10 c can be substantially similar to the assembly and deployment of the suture anchor 10 a discussed with regard to FIGS. 8-12 and the suture anchor 10 b discussed with regard to FIGS. 15 and 16, the assembly and deployment of the suture anchor 10 c will not be discussed in detail herein. Briefly, however, once the midsection 201 of the suture 30 a is coupled to the soft tissue 204 via the mattress stitch 206 or any other technique, such as a suture punch (not shown), the hand 86 of the operator can thread or insert the first end 200 and second end 202 of the suture 30 a through the aperture 266 of the necked portion 264 and into the throughbore 262 (not shown). Then, the suture anchor 10 c can be inserted into the pre-drilled hole 14. The hand 86 of the operator can be used to tighten the suture 30 a, and thus the soft tissue 204, to the pre-drilled hole 14 by pulling the first end 200 and second end 202 of the suture 30 a that extends from the pre-drilled hole 14 (not shown). This further removes any slack from the suture 30 a. After the suture 30 a is tightened, the expanding members 72 of the suture anchor 10 c can be deployed or expanded to engage the pre-drilled hole 14.

When the suture anchor 10 c is fully engaged to the pre-drilled hole 14, the tip 32 of the suture receiving portion 22 c can be adjacent to the suture 30 a, while the suture 30 a is adjacent to the first end 64 of the sleeve 20 (as best shown in FIG. 18). The compression of the suture 30 a between the suture receiving portion 22 c and the tip 32 can fix or lock the suture 30 a to the suture anchor 10 c. Thus, the suture anchor 10 c can also fix the suture 30 a to the suture anchor 10 c without the use of a knot. The first end 200 and second end 202 of the suture 30 a that extends from the pre-drilled hole 14 can then be trimmed if desired (not shown).

With reference to FIG. 19, a fourth alternative insert 18 d is shown. The fourth alternative insert 18 d can include a suture receiving portion 22 d, the breakaway section 26, and the end section 24 for use with a suture anchor 10 d substantially similar to that described with regard to FIGS. 7-12. As the breakaway section 26 and end section 24 of the fourth alternative insert 18 d are substantially similar to the breakaway section 26 and end section 24 of the insert 18, the breakaway section 26 and end section 24 will not be discussed in detail with regard to the fourth alternative insert 18 d. In addition, as the suture receiving portion 22 d is substantially similar to the suture receiving portion 22 a of the first alternative insert 18 a, as discussed with FIGS. 7-12, only the modifications to the suture receiving portion 22 d will be discussed herein.

As shown in FIG. 19, the suture receiving portion 22 d can include a hinged slot 270 which can be for receipt of the suture 30 a. Generally, the hinged slot 270 can be defined in a cylindrical body 34 d of the fourth alternative insert 18 d. As will be appreciated, the remainder of the cylindrical body 34 d can be generally similar to the cylindrical body 34 a that is illustrated in and described in conjunction with FIG. 7.

The hinged slot 270 can define a throughbore 272 and can include a hinged portion 274. The hinged portion 274 can optionally include at least one or a plurality of barbs or projections 276. The throughbore 272 can be configured to retain the first end 200 and second end 202 of the suture 30 a. The hinged portion 274 can be pivotably coupled to the cylindrical body 34 d and can rotate from an opened position to a closed position. In the opened position, as shown in FIG. 19, the hinged portion 274 can define an aperture 278 for receipt of the first end 200 and second end 202 of the suture 30 a to enable the suture 30 a to enter the throughbore 272 of the hinged slot 270. In the closed position, the hinged portion 274 can seal or enclose the aperture 278 to retain the suture 30 a within the throughbore 272, as shown in FIG. 20. Thus, generally, the hinged portion 274 can be sized such that in the closed position the hinged portion 274 can substantially enclose the aperture 278. The projections 276 of the hinged portion 274 are optional and can be coupled to or formed with the hinged portion 274 if desired. The projections 276 can extend into the throughbore 272 when the hinged portion 274 is in the closed position to further retain the suture 30 a within the throughbore 272. The projections 276 are illustrated as triangular, however, any appropriate shape, such as annular or hooked, could be employed.

As the assembly and deployment of the suture anchor 10 d in the pre-drilled hole 14 is substantially similar to the assembly and deployment of the suture anchor 10 a discussed with regard to FIGS. 8-12 and the suture anchor 10 b discussed with regard to FIGS. 15 and 16, the assembly and deployment of the suture anchor 10 d will not be discussed in detail herein. Briefly, however, once the midsection 201 of the suture 30 a is coupled to the soft tissue 204 via the mattress stitch 206 or any other technique, such as a suture punch, the hand 86 of the operator can thread or insert the first end 200 and second end 202 of the suture 30 a through the aperture 278 of the hinged portion 274 and into the throughbore 272 (not shown). Then, the suture anchor 10 d can be inserted into the pre-drilled hole 14 (not shown). The hand 86 of the operator can be used to tighten the suture 30 a, and thus the soft tissue 204, to the pre-drilled hole 14 by pulling the first end 200 and second end 202 of the suture 30 a that extends from the pre-drilled hole 14 (not shown). This further removes any slack from the suture 30 a. After the suture 30 a is tightened, the expanding members 72 of the suture anchor 10 d can be deployed to engage the pre-drilled hole 14. During the deployment of the suture anchor 10 d, as the fourth alternative insert 18 d moves rearwardly in the sleeve 20, the hinged portion 274 can be pushed closed by the sleeve 20 to lock the suture 30 a within the throughbore 272 of the suture receiving portion 22 d.

When the suture anchor 10 d is fully engaged to the pre-drilled hole 14, the tip 32 of the suture receiving portion 22 d can be adjacent to the suture 30 a, while the suture 30 a is adjacent to the first end 64 of the sleeve 20 (as best shown in FIG. 20). The compression of the suture 30 a between the suture receiving portion 22 d and the tip 32 can fix or lock the suture 30 a to the suture anchor 10 d. Thus, the suture anchor 10 d can also fix the suture 30 a to the suture anchor 10 d without the use of a knot. The first end 200 and second end 202 of the suture 30 a that extends from the pre-drilled hole 14 can then be trimmed if desired (not shown).

With reference to FIG. 21, a fifth alternative insert 18 e is shown. The fifth alternative insert 18 e can include a suture receiving portion 22 e, the breakaway section 26, and the end section 24 for use with a suture anchor 10 e substantially similar to that described with regard to FIGS. 1-6B. As will be appreciated, the remainder of the suture anchor 10 e can be generally similar to the suture anchor 10 that is illustrated in and described in conjunction with FIGS. 1-6B. As the breakaway section 26 and end section 24 of the fifth alternative insert 18 e are substantially similar to the breakaway section 26 and end section 24 of the insert 18, the breakaway section 26 and end section 24 will not be discussed in detail with regard to the fifth alternative insert 18 e.

The suture receiving portion 22 e and end section 24 can have a tensile and a torsion strength that are greater than the tensile and torsion strength of the breakaway section 26 such that the suture receiving portion 22 e and end section 24 will be severed by the breakaway section 26 without damage to the structural integrity of either section. The fifth alternative insert 18 e is generally insert molded from a resorbable material (such as, for example, Lactosorb® available from Biomet Inc. of Warsaw, Ind.); however, it will be understood that other types of biocompatible materials and other methods of forming could be used.

As shown in FIG. 21, the suture receiving portion 22 e can include the tip 32, a cylindrical body 34 e and a suture 30 e. The tip 32 can be generally conical in shape; however, any other desired shape may be used, such as rectangular. The cylindrical body 34 e can have a diameter D1 e, which is sized to ensure a slip fit with the sleeve 20 such that the cylindrical body 34 e can slide within the sleeve 20. The cylindrical body 34 e can define an aperture or eyelet 36 e extending through the cylindrical body 34 e to provide an attachment point for the suture 30 e. The cylindrical body 34 e can further include the tapered section 40 leading to the breakaway section 26.

With additional reference to FIGS. 22 and 23, the suture 30 e can have a first end 300, a midsection 302 and a second end 304. The first end 300 of the suture 30 e can be coupled to the breakaway section 26 of the fifth alternative insert 18 e. Generally, the first end 300 can be knotted about the breakaway section 26 at a midpoint 307 of the two necked portions 42, 44 (FIG. 22). The midsection 302 of the suture 30 e can be coupled to a section of soft tissue 306 (FIG. 23). The second end 304 of the suture 30 e can be received into the eyelet 36 e of the cylindrical body portion 34 e of the fifth alternative insert 18 e. The second end 304 can be coupled to a needle 309 (shown in phantom) to facilitate the threading of the second end 304 into the eyelet 36 e (FIG. 22). The second end 304, once threaded, can pass through the eyelet 36 e to secure the soft tissue 306 to the pre-drilled hole 14, as will be discussed in greater detail herein.

With reference to FIG. 23, prior to the assembly of the sleeve 20 with the fifth alternative insert 18 e, the first end 300 of the suture 30 e can be knotted to the midpoint 307 of the breakaway section 26 of the fifth alternative insert 18 e. Then, the sleeve 20 can be disposed over the breakaway section 26 of the fifth alternative insert 18 e, such that the second end 304 of the suture 30 e can extend out from the sleeve 20. Then, with the pre-drilled hole 14 drilled into the boney structure 16, and the first end the suture 30 e coupled to the breakaway section 26, the midsection 302 of the suture 30 e can be coupled to the soft tissue 306. The suture 30 e can be coupled to the soft tissue 306 through any appropriate technique, such as a mattress stitch 308 or a suture punch (not shown), for example. Then, the hand 86 of an operator can thread or insert the second end 304 of the suture 30 e through the eyelet 36 e with or without the use of the needle 309.

With additional reference to FIG. 24, once the second end 304 of the suture 30 e is threaded through the eyelet 36 e, the suture anchor 10 e can be inserted into the pre-drilled hole 14. Generally, the second end 304 of the suture 30 e can extend beyond the pre-drilled hole 14 to enable the hand 86 of the operator to grasp the second end 304 to tighten the suture 30 e, and thus the soft tissue 306, to the pre-drilled hole 14. Typically, the suture 30 e can be tightened by pulling the second end 304 of the suture 30 e that extends beyond the pre-drilled hole 14. This further removes any slack from the suture 30 e. After the suture 30 e is tightened, the expanding members 72 of the suture anchor 10 e can be deployed to engage the pre-drilled hole 14.

As discussed herein, the alternative alternative syringe-type actuator 88′ can be used to expand the expanding members 72 of the suture anchor 10 e; however, any other activating device, such as the actuator gun 56 discussed with regard to FIGS. 4A and 4B, or the syringe-type actuator 88 discussed with regard to FIG. 4D, could be used. If the alternative alternative syringe-type actuator 88′ is used, then the lever 92′ on the alternative syringe-type actuator 88′ can be pulled, as shown in FIG. 25, to apply the retractive force F1 to the actuator pin 12. The application of the retractive force F1 can cause the fifth alternative insert 18 e to be displaced or moved rearwardly with respect to the sleeve 20 and can cause the tapered portion 46 of the fifth alternative insert 18 e to apply a force F3 to the tapered interior bearing surface 80 of the expanding members 72 of the sleeve 20 until the expanding members 72 are engaged with the boney structure 16.

When the expanding members 72 are fully engaged, the tip 32 of the suture receiving portion 22 e can be adjacent to the suture 30 e, while the suture 30 e is adjacent to the first end 64 of the sleeve 20 (as best shown in FIG. 19). The compression of the suture 30 e between the suture receiving portion 22 e and the tip 32 can fix or lock the suture 30 e to the suture anchor 10 e, while preventing the fifth alternative insert 18 e from retracting further. The continued application of the retractive force F1 to the fifth alternative insert 18 e can cause the breakaway section 26 to fracture, as shown in FIG. 26. Once the breakaway section 26 fractures, the sleeve 20 and suture receiving portion 22 e remain in the pre-drilled hole 14 to couple the soft tissue 306 to the boney structure 16 via the suture 30 e. The portion of the second end 304 that extends from the pre-drilled hole 14 can then be trimmed if desired (not shown).

As shown in FIG. 27, the suture anchor 10 e can fix or lock the second end 304 of the suture 30 e to the suture anchor 10 e without the use of a knot. In addition, the suture anchor 10 e can ensure the first end 300 of the suture 30 e remains fixed to the fifth alternative insert 18 e. Generally, as a portion of the first end 300 extends from the sleeve 20 and the second end 304 extends from the eyelet 36 e of the fifth alternative insert 18 e prior to the deployment of the expanding members 72 of the sleeve 20, the application of the retractive force F1 causes the fifth alternative insert 18 e, and thus the portion of the first end 300 and the second end 304 extending from the eyelet 36 e, to be withdrawn into the sleeve 20. Thus, the movement of the fifth alternative insert 18 e within the sleeve 20 can fix or lock the portion of the first end 300 and the second end 304 to the suture anchor 10 e due to the interference fit between the fifth alternative insert 18 e, the suture 30 e, and the sleeve 20, as discussed previously. Additionally, the frictional lock created between the suture 30 e, the fifth alternative insert 18 e and the sleeve 20 can prevent the fifth alternative insert 18 e from moving after the deployment of the expanding members.

With reference to FIG. 28, a sixth alternative insert 18 f is shown. The sixth alternative insert 18 f can include a suture receiving portion 22 f, the breakaway section 26, and the end section 24 for use with a suture anchor 10 f substantially similar to the suture anchor 10 e described with regard to FIGS. 21-27. As the breakaway section 26 and end section 24 of the sixth alternative insert 18 f are substantially similar to the breakaway section 26 and end section 24 of the insert 18, the breakaway section 26 and end section 24 will not be discussed in detail with regard to the sixth alternative insert 18 f. In addition, as the suture receiving portion 22 f is substantially similar to the suture receiving portion 22 e of the fifth alternative insert 18 e, as discussed with reference to FIGS. 21-27, only the modifications to the suture receiving portion 22 f will be discussed herein.

As shown in FIG. 28, the suture receiving portion 22 f can include an aperture, for example, a groove or slot 350, which can be for receipt of the suture 30 e. Generally, the slot 350 can be formed longitudinally in a cylindrical body 34 f of the sixth alternative insert 18 f; however, the slot 350 can be formed in any desired position, such as vertically or diagonally. As will be appreciated, the remainder of the cylindrical body 34 f can be generally similar to the cylindrical body 34 e that is illustrated in and described in conjunction with FIG. 21.

The slot 350 can extend for a length L and can have a height H configured to enable an operator to insert the second end 304 of the suture 30 e through the slot 350, as shown in FIG. 29. Generally, once the first end 300 of the suture 30 e is tied to the breakaway section 26 and the midsection 302 of the suture 30 e is coupled to the soft tissue 306 via the mattress stitch 308 or any other technique, such as a suture punch (not shown), the hand 86 of the operator can thread or insert the second end 304 of the suture 30 e into the slot 350.

With reference to FIG. 30, the suture anchor 10 f can be inserted into the pre-drilled hole 14 formed in the boney structure 16. Next, as discussed herein, the hand 86 of the operator can be used to tighten the suture 30 e, and thus the soft tissue 306, to the pre-drilled hole 14 by pulling the second end 304 of the suture 30 e that extends from the pre-drilled hole 14. After the suture 30 e is tightened, the expanding members 72 of the suture anchor 10 f can be expanded to engage the pre-drilled hole 14 through the use of the actuator gun 56, syringe-type actuator 88 or syringe-type actuator 88′, for example, as discussed previously with reference to FIGS. 4A and 4B, 4D and 9-12, respectively.

When the suture anchor 10 f is fully engaged to the pre-drilled hole 14, the tip 32 of the suture receiving portion 22 f can be adjacent to the suture 30 e, while the suture 30 e is adjacent to the first end 64 of the sleeve 20, as best shown in FIG. 31. The compression of the suture 30 e between the suture receiving portion 22 f and the tip 32 can fix or lock the suture 30 e to the suture anchor 10 f. Thus, the suture anchor 10 f can fix the second end 304 of the suture 30 e to the suture anchor 10 f without the use of a knot, while providing greater access for the operator to couple the second end 304 of the suture 30 e to the sixth alternative insert 18 f prior to the insertion of the suture anchor 10 f into the pre-drilled hole 14. The portion of the second end 304 that extends from the pre-drilled hole 14 can then be trimmed if desired (not shown).

With reference to FIG. 32, a seventh alternative insert 18 g is shown. The seventh alternative insert 18 g can include a suture receiving portion 22 g, the breakaway section 26, and the end section 24 for use with a suture anchor 10 g substantially similar to the suture anchor 10 e described with regard to FIGS. 21-27. As the breakaway section 26 and end section 24 of the seventh alternative insert 18 g are substantially similar to the breakaway section 26 and end section 24 of the insert 18, the breakaway section 26 and end section 24 will not be discussed in detail with regard to the seventh alternative insert 18 g. In addition, as the suture receiving portion 22 g is substantially similar to the suture receiving portion 22 e of the fifth alternative insert 18 e, as discussed with FIGS. 21-27, only the modifications to the suture receiving portion 22 g will be discussed herein.

As shown in FIG. 32, the suture receiving portion 22 g can include a slot, for example, a C-shaped slot 360, which can be for receipt of the suture 30 e. Generally, the slot 360 can be defined in a cylindrical body 34 g of the seventh alternative insert 18 g. As will be appreciated, the remainder of the cylindrical body 34 g can be generally similar to the cylindrical body 34 e that is illustrated in and described in conjunction with FIG. 21. The slot 360 can define a throughbore 362 and a necked portion 364. The necked portion 364 can define an aperture 366 for receipt of the first end 300 and second end 304 of the suture 30 e. Generally, the necked portion 364 can be configured such that the first end 300 and second end 304 of the suture 30 e can be hooked behind and retained by the necked portion 364.

As the assembly and deployment of the suture anchor 10 g in the pre-drilled hole 14 is substantially similar to the deployment of the suture anchor 10 e discussed with regard to FIGS. 21-27 and the suture anchor 10 f discussed with regard to FIGS. 30 and 31, the assembly and deployment of the suture anchor 10 g will not be discussed in detail herein. Briefly, however, the first end 300 of the suture 30 e can be tied to the breakaway section 26 and the midsection 302 of the suture 30 e can be coupled to the soft tissue 306 via the mattress stitch 308 or any other technique, such as a suture punch (not shown). Then, the hand 86 of the operator can thread or insert the second end 304 of the suture 30 e into the slot 360 (not shown). Then, the suture anchor 10 g can be inserted into the pre-drilled hole 14 and the hand 86 of the operator can be used to tighten the suture 30 e, and thus the soft tissue 306, to the pre-drilled hole 14 by pulling the second end 304 of the suture 30 e that extends from the pre-drilled hole 14 (not shown). This further removes any slack from the suture 30 e. After the suture 30 e is tightened, the expanding members 72 of the suture anchor 10 g can be deployed to engage the pre-drilled hole 14.

When the suture anchor 10 g is fully engaged to the pre-drilled hole 14, the tip 32 of the suture receiving portion 22 g can be adjacent to the suture 30 e, while the suture 30 e is adjacent to the first end 64 of the sleeve 20, as best shown in FIG. 33. The compression of the suture 30 e between the suture receiving portion 22 g and the tip 32 can fix or lock the suture 30 e to the suture anchor 10 g. Thus, the suture anchor 10 g can fix the second end 304 of the suture 30 e to the suture anchor 10 g without the use of a knot, while providing greater access for the operator to couple the second end 304 of the suture 30 e to the seventh alternative insert 18 g prior to the insertion of the suture anchor 10 g into the pre-drilled hole 14. The portion of the second end 304 that extends from the pre-drilled hole 14 can then be trimmed if desired (not shown).

With reference to FIG. 34, an eighth alternative insert 18 h is shown. The eighth alternative insert 18 h can include a suture receiving portion 22 h, the breakaway section 26, and the end section 24 for use with a suture anchor 10 h substantially similar to the suture anchor 10 e described with regard to FIGS. 21-27. As the breakaway section 26 and end section 24 of the eighth alternative insert 18 h are substantially similar to the breakaway section 26 and end section 24 of the insert 18, the breakaway section 26 and end section 24 will not be discussed in detail with regard to the eighth alternative insert 18 h. In addition, as the suture receiving portion 22 h is substantially similar to the suture receiving portion 22 e of the fifth alternative insert 18 e, as discussed with FIGS. 21-27, only the modifications to the suture receiving portion 22 h will be discussed herein.

As shown in FIG. 34, the suture receiving portion 22 h can include a hinged slot 370 which can be for receipt of the suture 30 e. Generally, the hinged slot 370 can be defined in a cylindrical body 34 h of the eighth alternative insert 18 h. As will be appreciated, the remainder of the cylindrical body 34 h can be generally similar to the cylindrical body 34 e that is illustrated in and described in conjunction with FIG. 21.

The hinged slot 370 can define a throughbore 372 and can include a hinged portion 374. The hinged portion 374 can optionally include at least one or a plurality of barbs or projections 376. The throughbore 372 can be configured to retain the first end 300 and second end 304 of the suture 30 e. The hinged portion 374 can be pivotably coupled to the cylindrical body 34 h and can rotate from an opened position to a closed position. In the opened position, as shown in FIG. 34, the hinged portion 374 can define an aperture 378 for receipt of the first end 300 and second end 304 of the suture 30 e to enable the suture 30 e to enter the throughbore 372 of the hinged slot 370. In the closed position, the hinged portion 374 can substantially enclose the aperture 378 to retain the suture 30 e within the throughbore 372, as shown in FIG. 35. Thus, generally, the hinged portion 374 can be sized such that in the closed position the hinged portion 374 can substantially enclose the aperture 378. The projections 376 are optional and can be coupled to or formed with the hinged portion 374 if desired. The projections 376 can extend into the throughbore 372 when the hinged portion 374 is in the closed position to further retain the suture 30 e within the throughbore 372. The projections 376 are illustrated as triangular, however, any appropriate shape, such as annular or hooked, could be employed.

As the assembly and deployment of the suture anchor 10 h in the pre-drilled hole 14 is substantially similar to the assembly and deployment of the suture anchor 10 e discussed with regard to FIGS. 21-27 and the suture anchor 10 f discussed with regard to FIGS. 30 and 31, the assembly and deployment of the suture anchor 10 h will not be discussed in detail herein. Briefly, however, the first end 300 of the suture 30 e can be tied to the breakaway section 26 and the midsection 302 of the suture 30 e can be coupled to the soft tissue 306 via the mattress stitch 308 or any other technique, such as a suture punch (not shown). The hand 86 of the operator can thread or insert the second end 304 of the suture 30 e into the hinged slot 370 (not shown). Then, the suture anchor 10 h can be inserted into the pre-drilled hole 14 and the hand 86 of the operator can be used to tighten the suture 30 e, and thus the soft tissue 306, to the pre-drilled hole 14 by pulling the second end 304 of the suture 30 e that extends from the pre-drilled hole 14 (not shown). This further removes any slack from the suture 30 e. After the suture 30 e is tightened, the expanding members 72 of the suture anchor 10 h can be deployed to engage the pre-drilled hole 14. During the deployment of the suture anchor 10 h, as the eighth alternative insert 18 h moves rearwardly in the sleeve 20, the hinged portion 374 can be pushed closed by the sleeve 20 to lock the suture 30 e within the throughbore 372 of the suture receiving portion 22 h.

When the suture anchor 10 h is fully engaged to the pre-drilled hole 14, the tip 32 of the suture receiving portion 22 h can be adjacent to the suture 30 e, while the suture 30 e is adjacent to the first end 64 of the sleeve 20, as best shown in FIG. 35. The compression of the suture 30 e between the suture receiving portion 22 h and the tip 32 can fix or lock the suture 30 e to the suture anchor 10 h. Thus, the suture anchor 10 h can also fix the second end 304 of the suture 30 e to the suture anchor 10 h without the use of a knot. The portion of the second end 304 that extends from the pre-drilled hole 14 can then be trimmed if desired (not shown).

With reference to FIG. 36, a ninth alternative insert 18 i is shown. The ninth alternative insert 18 i can include a suture receiving portion 22 i, the breakaway section 26, and the end section 24 for use with a suture anchor 10 i substantially similar to the suture anchor 10 described with regard to FIGS. 1-7. As the breakaway section 26 and end section 24 of the ninth alternative insert 18 i are substantially similar to the breakaway section 26 and end section 24 of the insert 18, the breakaway section 26 and end section 24 will not be discussed in detail with regard to the ninth alternative insert 18 i. In addition, as the suture receiving portion 22 i is substantially similar to the suture receiving portion 22 of the insert 18, as discussed with FIGS. 1-6B, only the modifications to the suture receiving portion 22 i will be discussed herein.

As shown in FIG. 36, the suture receiving portion 22 i includes the eyelet 36 and a hinged slot 400. Generally, the eyelet 36 and hinged slot 400 can each be defined in a cylindrical body 34 i of the ninth alternative insert 18 i. As will be appreciated, the remainder of the cylindrical body 34 i can be generally similar to the cylindrical body 34 that is illustrated in and described in conjunction with FIGS. 1-6B. The eyelet 36 can be configured for receipt of the suture 30 therein, as discussed herein, while the hinged slot 400 can be configured for receipt of a suture 30 i therein.

The hinged slot 400 can include a throughbore 402, a first hinged portion 404 and a second hinged portion 406. The throughbore 402 defines a passageway for receipt of the suture 30 i therethrough and can include a first end 408 and a second end 410. The first hinged portion 404 can be pivotably coupled to the first end 408 of the throughbore 402 and the second hinged portion 406 can be pivotably coupled to the second end 410 of the throughbore 402. The first hinged portion 404 and second hinged portion 406 can generally be pivotable from an opened position to a closed position. In the opened position, as shown in FIG. 36, the first hinged portion 404 and second hinged portion 406 can enable the suture 30 i to be received into and through the throughbore 402. In the closed position, as shown in FIG. 37, the first hinged portion 404 and second hinged portion 406 can generally pivot to enclose the first end 408 and second end 410 of the throughbore 402, respectively, to secure or lock the suture 30 i within the throughbore 402. Thus, generally, the first hinged portion 404 and the second hinged portion 406 can be sized to create an interference fit between the suture 30 i, the first and second hinged portion 404, 406 and the throughbore 402 to lock the suture 30 i to the ninth alternative insert 18 i.

The suture 30 i can include a first end 412, a midsection 414 and a second end 416. The suture 30 i can be used to couple multiple suture anchors 10 together, wherein the reference numeral “10” denotes all of the suture anchors 10. Generally, the first end 412 of the suture 30 i can be coupled to an adjacent suture anchor 10 (not specifically shown) and the midsection 414 of the suture 30 i can pass through the throughbore 402 to secure the suture 30 i to the suture anchor 10 i. The second end 416 of the suture 30 i can then be coupled to another suture anchor 10, or can be trimmed. Alternatively, the midsection 414 of the suture 30 i can be coupled to additional soft tissue (not shown). If the midsection 414 is coupled to additional soft tissue, then the first end 412 and second end 416 of the suture 30 i can pass through the throughbore 402 to couple the additional soft tissue to the suture anchor 10, as shown in FIG. 36A.

As the assembly and deployment of the suture anchor 10 i in the pre-drilled hole 14 is substantially similar to the deployment of the suture anchor 10 discussed with regard to FIGS. 4A-6B and the suture anchor 10 a discussed with regard to FIGS. 8-12, the assembly and deployment of the suture anchor 10 i will not be discussed in detail herein. Briefly, however, in order to employ the suture anchor 10 i, the suture 30 can be threaded through the eyelet 36 of the ninth alternative insert 18 i and then the sleeve 20 can be disposed over the ninth alternative insert 18 i (not specifically shown). The suture 30 i can then be coupled to an adjacent suture anchor 10 or to the additional soft tissue via a mattress stitch or any other technique, such as a suture punch (not shown). If the suture 30 i is coupled to an adjacent suture anchor 10, then the hand 86 of the operator can thread or insert the second end 416 of the suture 30 e into the throughbore 402 until the midsection 414 is received in the throughbore 402 of hinged slot 400, and the second end 416 of the suture 30 i extends beyond the second end 410 of the throughbore 402. If the suture 30 i is coupled to the additional soft tissue, then the hand 86 of the operator can thread or insert the first end 412 and the second end 416 of the suture 30 i into the hinged slot 400 (not shown). Once the suture 30 i is threaded through the hinged slot 400, the suture anchor 10 i can be inserted into the pre-drilled hole 14.

The hand 86 of the operator can be used to tighten the suture 30 i to the pre-drilled hole 14 by pulling the respective first end 414 and/or second end 416 of the suture 30 i that extends from the pre-drilled hole 14. This further removes any slack from the suture 30 i (not shown). After the suture 30 i is tightened, the expanding members 72 of the suture anchor 10 i can be deployed to engage the pre-drilled hole 14. During the deployment of the suture anchor 10 i, as the ninth alternative insert 18 i moves rearwardly in the sleeve 20, the first hinged portion 404 and second hinged portion 406 can be pushed closed by the sleeve 20 to lock the suture 30 i within the throughbore 402 of the suture receiving portion 22 i as shown in FIGS. 37 and 37B. In addition, if necessary, the suture 30 coupled to the eyelet 36 can be pulled by the hand 86 of the operator to fully expand the expanding members 72 in soft boney tissue, as discussed herein.

When the suture anchor 10 i is fully engaged to the pre-drilled hole 14, the tip 32 of the suture receiving portion 22 i can be adjacent to the suture 30 i, while the suture 30 i is adjacent to the first end 64 of the sleeve 20, as best shown in FIGS. 37 and 37B. The compression of the suture 30 i between the suture receiving portion 22 i and the tip 32 can fix or lock the suture 30 i to the suture anchor 10 i. Thus, the suture anchor 10 i can fix the first end 412 (FIG. 37), and the first end 412 and the second end 416 (FIG. 37B) of the suture 30 i to the suture anchor 10 i without the use of a knot. The portion of the first end 412 and/or second end 416 that extends from the pre-drilled hole 14 can then be trimmed if desired (not shown).

With reference to FIG. 38, a tenth alternative insert 18 j is shown. The tenth alternative insert 18 j can include a suture receiving portion 22 j, the breakaway section 26, and the end section 24 for use with a suture anchor 10 j substantially similar to the suture anchor 10 described with regard to FIGS. 1-6B. As the breakaway section 26 and end section 24 of the tenth alternative insert 18 j are substantially similar to the breakaway section 26 and end section 24 of the insert 18, the breakaway section 26 and end section 24 will not be discussed in detail with regard to the tenth alternative insert 18 j. In addition, as the suture receiving portion 22 j is substantially similar to the suture receiving portion 22 of the insert 18, as discussed with FIGS. 1-6B, only the modifications to the suture receiving portion 22 j will be discussed herein.

As shown in FIG. 36, the suture receiving portion 22 j includes the eyelet 36 and a second formed eyelet 450. Generally, the eyelet 36 and second formed eyelet 450 can each be defined in a cylindrical body 34 j of the tenth alternative insert 18 j. As will be appreciated, the remainder of the cylindrical body 34 j can be generally similar to the cylindrical body 34 that is illustrated in and described in conjunction with FIGS. 1-6B. The eyelet 36 can be configured for receipt of the suture 30 therein, as discussed previously, while the second formed eyelet 450 can be configured for receipt of the suture 30 j therein.

The second formed eyelet 450 can generally be formed perpendicular to the eyelet 36; however, the second formed eyelet 450 could be formed in any appropriate orientation with regard to the eyelet 36, such as parallel. The second formed eyelet 450 defines a passageway for receipt of a suture 30 j therethrough. The suture 30 j can be used to couple multiple suture anchors 10 together, wherein the reference numeral “10” denotes all of the suture anchors 10, or the suture 30 j can be used to couple additional soft tissue to the suture anchor 10 j. The suture 30 j can include a first end 418, a midsection 420 and a second end 422. The midsection 420 can be coupled to either the suture anchor 10 or additional soft tissue, while the first end 418 and second end 422 can pass through the second formed eyelet 450 to couple the suture 30 j to the suture anchor 10 j.

As the assembly and deployment of the suture anchor 10 j in the pre-drilled hole 14 is substantially similar to the assembly and deployment of the suture anchor 10 discussed with regard to FIGS. 4A-6B and the suture anchor 10 a discussed with regard to FIGS. 8-12, the assembly and deployment of the suture anchor 10 j will not be discussed in detail herein. Briefly, however, in order to employ the suture anchor 10 j, the suture 30 can be threaded through the eyelet 36 of the tenth alternative insert 18 j and then the sleeve 20 can be disposed over the tenth alternative insert 18 j (not specifically shown). The suture 30 j can then be coupled to an adjacent suture anchor 10 or to additional soft tissue via the mattress stitch or any other technique, such as a suture punch (not shown).

If the suture 30 j is coupled to an adjacent suture anchor 10, then the hand 86 of the operator can thread or insert the second end 416 of the suture 30 j into the second formed eyelet 450 until the midsection 414 is received in the second formed eyelet 450, and the second end 416 of the suture 30 j extends beyond the suture anchor 10 j. If the suture 30 i is coupled to the additional soft tissue, then the hand 86 of the operator can thread or insert the first end 412 and the second end 416 of the suture 30 j into the second formed eyelet 450 (not shown). Once the suture 30 j is threaded through the second formed eyelet 450, the suture anchor 10 j can be inserted into the pre-drilled hole 14.

As discussed herein, the hand 86 of the operator can be used to tighten the suture 30 j to the pre-drilled hole 14 by pulling the first end 418 and second end 416 of the suture 30 j that extends from the pre-drilled hole 14 (not shown). After the suture 30 j is tightened, the expanding members 72 of the suture anchor 10 j can be deployed to engage the pre-drilled hole 14. It should be noted, however, that if necessary, the suture 30 coupled to the eyelet 36 can be pulled by a hand 86 of an operator to fully expand the expanding members 72, as discussed herein.

When the suture anchor 10 j is fully engaged to the pre-drilled hole 14, the tip 32 of the suture receiving portion 22 j can be adjacent to the suture 30 j, while the suture 30 j is adjacent to the first end 64 of the sleeve 20, as best shown in FIG. 39. The compression of the suture 30 j between the suture receiving portion 22 j and the tip 32 can fix or lock the suture 30 j to the suture anchor 10 j. Thus, the suture anchor 10 j can fix the first end 412 and second end 416 of the suture 30 j to the suture anchor 10 j without the use of a knot. The portion of the first end 412 and second end 416 of the suture 30 j that extends from the pre-drilled hole 14 can then be trimmed if desired (not shown).

With reference to FIG. 40, an eleventh alternative insert 18 k is shown. The eleventh alternative insert 18 k can include a suture receiving portion 22 k, the breakaway section 26, and the end section 24 for use with a suture anchor 10 k substantially similar to the suture anchor 10 e described with regard to FIGS. 21-27. As the breakaway section 26 and end section 24 of the eleventh alternative insert 18 k are substantially similar to the breakaway section 26 and end section 24 of the insert 18, the breakaway section 26 and end section 24 will not be discussed in detail with regard to the eleventh alternative insert 18 k. In addition, as the suture receiving portion 22 k is substantially similar to the suture receiving portion 22 e of the fifth alternative insert 18 e, as discussed with FIGS. 21-27, only the modifications to the suture receiving portion 22 k will be discussed herein.

As shown in FIG. 40, the suture receiving portion 22 k can include the eyelet 36 and a second formed eyelet 460. Generally, the eyelet 36 and second formed eyelet 460 can each be defined in a cylindrical body 34 k of the eleventh alternative insert 18 k. As will be appreciated, the remainder of the cylindrical body 34 k can be generally similar to the cylindrical body 34 that is illustrated in and described in conjunction with FIGS. 1-6B. The eyelet 36 can be configured for receipt of a suture 30′ therein, while the second formed eyelet 460 can be configured for receipt of the suture 30 k therein. The suture 30′ can include a first end 454, a midsection 456 and second end 458. The first end 454 of the suture 30′ can be coupled to a suture anchor 10 or additional soft tissue 462 and can pass through the second formed eyelet 460 to couple the suture 30′ to the suture anchor 10 k. The midsection 456 can be received through the eyelet 36 to further retain the suture 30′ within the suture anchor 10 k. The second end 458 can extend from the second end 66 of the sleeve 20.

The second formed eyelet 460 can generally be formed perpendicular to the eyelet 36; however, the second formed eyelet 460 could be formed in any appropriate orientation with regard to the eyelet 36, such as parallel. The second formed eyelet 460 defines a passageway for receipt of the suture 30 k therethrough. The suture 30 k can be used to couple multiple suture anchors 10 together, wherein the reference numeral “10” denotes all of the suture anchors 10, or the suture 30 k can be used to couple additional soft tissue 462 to the suture anchor 10 k. The suture 30 k can include a first end 464, a midsection 466, and a second end 468. The first end 464 can be coupled to the breakaway section 26 of the eleventh alternative insert 18 k. The midsection 466 can be coupled to either the suture anchor 10 or to the additional soft tissue 462. The second end 468 of the suture 30 k can pass through the second formed eyelet 460 to couple the suture 30 k to the suture anchor 10 k.

Typically, in order to employ the suture anchor 10 k, with additional reference to FIG. 41, the suture 30′ can be threaded through the eyelet 36 of the eleventh alternative insert 18 k and then the first end 412 of the suture 30 k can be tied to the breakaway section 26. The sleeve 20 can be disposed over the eleventh alternative insert 18 k such that the suture 30′ and the suture 30 k extend from the second end 66 of the sleeve 20. Then, the midsection 466 of the suture 30 k and a portion 470 of the first end 454 of the suture 30′ can then be coupled to an adjacent suture anchor 10 (not shown) or to the additional soft tissue 462 via the mattress stitch 472 or any other technique, such as a suture punch. If the suture 30′ and the suture 30 k are coupled to an adjacent suture anchor 10, then the hand 86 of the operator can thread or insert the first end 454 of the suture 30′ and the second end 468 of the suture 30 k into the second formed eyelet 460 until the first end 454 of the suture 30′ and the second end 468 of the suture 30 k extend beyond the suture anchor 10 k (not shown).

If the midsection 466 of the suture 30 k and the portion 470 of the first end 454 of the suture 30′ are coupled to the additional soft tissue 462, then the hand 86 of the operator can thread or insert the first end 454 of the suture 30′ and the second end 468 of the suture 30 k into the second formed eyelet 460, as shown in FIG. 41. Once the first end 454 of the suture 30′ and the suture 30 k are threaded through the second formed eyelet 460, the suture anchor 10 k can be inserted into the pre-drilled hole 14.

The hand 86 of the operator can be used to tighten the additional soft tissue 462 to the pre-drilled hole 14 by pulling the suture 30 k and the first end 454 of the suture 30′ that extends from the pre-drilled hole 14. After the suture 30′ and suture 30 k are tightened, the expanding members 72 of the suture anchor 10 k can be deployed to engage the pre-drilled hole 14. As the deployment of the suture anchor 10 k in the pre-drilled hole 14 is substantially similar to the deployment of the suture anchor 10 discussed with regard to FIGS. 4A-6B and the suture anchor 10 e discussed with regard to FIGS. 21-27, the deployment of the suture anchor 10 k will not be discussed in detail herein. It should be noted, however, that if necessary, the first end 454 and second end 458 of the suture 30′ coupled to the eyelet 36 can be pulled by the hand 86 of the operator to fully expand the expanding members 72 in the case of soft boney tissue, as discussed herein.

When the suture anchor 10 k is fully engaged to the pre-drilled hole 14, the tip 32 of the suture receiving portion 22 k can be adjacent to the suture 30′ and the suture 30 k, while the suture 30′ and suture 30 k are adjacent to the first end 64 of the sleeve 20, as best shown in FIG. 42. The compression of the suture 30′ and the suture 30 k between the suture receiving portion 22 k and the tip 32 can fix or lock the suture 30′ and the suture 30 k to the suture anchor 10 k. Thus, the suture anchor 10 k can fix the suture 30′ and the suture 30 k to the suture anchor 10 k without the use of a knot. The portion of the second end 458 of the suture 30′ and the suture 30 k that extend from the pre-drilled hole 14 can then be trimmed if desired (not shown).

The description of these teachings is merely exemplary in nature and, thus, variations that do not depart from the gist of the teachings are intended to be within the scope of the teachings. Such variations are not to be regarded as a departure from the spirit and scope of the teachings. 

What is claimed is:
 1. A suture anchor system for attaching soft tissue to a boney structure comprising: an anchor including external threads for engaging the boney structure; an insert defining an aperture and configured to be slideably coupled to the anchor, the insert including a tip having a shoulder, the shoulder including a shelf surface at a proximal side of the shoulder, wherein the insert is configured to receive the anchor over a proximal end of the insert such that a distal end of the anchor is prevented from further advancing over the insert in a distal direction by the shelf surface of the shoulder; a suture received in the aperture, the suture adapted to be coupled to the soft tissue; and an anchor implanting tool removably engaging the insert and the anchor such that the anchor implanting tool is configured to implant the insert into the boney structure and then position the anchor over the insert such that the distal end of the anchor is advanced over a proximal end of the insert, wherein the insert and the anchor are configured to compress the suture between the distal end of the anchor and the shelf surface of the shoulder to lock the suture relative to the anchor without the use of a knot, wherein the external threads are configured to engage the suture.
 2. The suture anchor system of claim 1, wherein the anchor further comprises: a sleeve disposed around at least a portion of the insert, wherein the sleeve includes at least one expanding member for engaging the boney structure when the insert is moved.
 3. The suture anchor system of claim 2, wherein the insert further comprises: a breakaway section; a tapered section adjacent to the breakaway section; and a metallic member molded to the insert, the metallic member for moving the insert, wherein the sleeve is disposed around the aperture, the breakaway section and the tapered section of the insert and the metallic member is molded to the tapered section of the insert.
 4. The suture anchor system of claim 3, wherein the sleeve further includes: an inner bore defining a tapered section, wherein the at least one expanding member defines the tapered section of the inner bore and disposed adjacent to the breakaway section of the insert.
 5. The suture anchor system of claim 4, wherein the at least one expanding member is activated by a retractive force applied to the metallic member, the retractive force for causing the insert to move within the sleeve to expand the at least one expanding member.
 6. The suture anchor system of claim 5, wherein the movement of the insert causes the tapered section of the insert to contact the tapered portion of the sleeve to force the at least one expanding member to expand.
 7. The suture anchor system of claim 6, wherein the suture further comprises: a first end coupled to the breakaway section; a second end received in the aperture; and a midsection adapted to be coupled to the soft tissue, wherein the movement of the insert in the sleeve fixes the second end of the suture within the sleeve without the use of a knot.
 8. The suture anchor system of claim 6, wherein the suture further comprises: a first end received in the aperture; a second end received in the aperture; and a midsection adapted to be coupled to the soft tissue, wherein the movement of the insert in the sleeve fixes the first end and the second end of the suture within the sleeve without the use of a knot.
 9. The suture anchor system of claim 1, wherein the aperture is a slot.
 10. The suture anchor system of claim 1, wherein the aperture is an eyelet.
 11. The suture anchor system of claim 1, wherein the anchor is configured to be positioned over at least a portion of the insert such that the suture is fixed to the anchor without the use of a knot.
 12. The suture anchor system of claim 1, wherein the aperture includes a hinged portion that is pivotable between a first opened position and a second closed position, wherein in the second closed position, the hinged portion retains the suture relative to the aperture.
 13. The suture anchor system of claim 1, wherein the aperture includes a first eyelet passing through the insert and a second eyelet passing through the insert, wherein the first eyelet is positioned substantially perpendicular to and spaced apart from the second eyelet.
 14. A suture anchor system for attaching soft tissue to a boney structure, comprising: a sleeve extending from a proximal end to a distal end and including threads on an external surface configured to engage the boney structure; an insert configured to be positioned within the sleeve, the insert having a tip and a suture receiving portion configured to receive a suture; and an anchor implanting tool removably engaging the insert and the sleeve such that the anchor implanting tool is configured to implant the insert into the boney structure and then position the sleeve over the insert in a proximal to distal direction, wherein positioning the sleeve over the insert compresses the suture between the tip and the suture receiving portion to fix the suture to the suture anchor without a knot, wherein the external threads are configured to engage the suture.
 15. The suture anchor system of claim 14, wherein the tip defines a shoulder relative to the suture receiving portion, wherein upon positioning of the sleeve over the insert, the suture is compressed between the shoulder of the tip and the distal end of the sleeve.
 16. The suture anchor system of claim 15, wherein the sleeve comprises at least one expanding member defined by a U-shaped slot formed in a mid-section of the sleeve so as to be spaced apart from the proximal end and the distal end of the sleeve where the U-shaped slot defines three sides of a periphery of the expanding member with a fourth side of the periphery of the expanding member hingeably coupled to the mid-section of the sleeve.
 17. The suture anchor system of claim 14, wherein the suture receiving portion includes a hinged portion configured to be moved between an open position and a closed position, wherein in the closed position, the hinge portion is configured to retain the suture relative to the insert.
 18. The suture anchor system of claim 14, wherein the suture receiving portion defines a bore passing through the insert, where the bore includes a first hinged portion at a first end of the bore and a second hinged portion at a second end of the bore.
 19. The suture anchor system of claim 14, wherein the suture receiving portion includes a C-shaped slot defined by the insert, where the C-shaped slot has a through bore and a necked portion.
 20. A suture anchor system for attaching soft tissue to a boney structure, comprising: a sleeve extending from a proximal end to a distal end and including threads on an outer surface configured to engage a suture and the boney structure; an insert, wherein the insert and the sleeve are movable relative to each other, such that the sleeve can be positioned over a proximal portion of the insert from a proximal to distal direction, the insert having a tip and a suture receiving portion; and an anchor implanting tool removably engaging the insert and the sleeve such that the anchor implanting tool is configured to implant the insert into the boney structure and then position the sleeve over the insert in the proximal to distal direction, wherein positioning the sleeve over the insert compresses the suture between the tip and the distal end of the sleeve to fix the suture to the suture anchor without a knot.
 21. The suture anchor system of claim 20, wherein the suture receiving portion includes a bore having a hinge portion configured to retain a suture in the bore.
 22. The suture anchor system of claim 21, wherein the hinged portion includes barbs configured to engage the suture.
 23. The suture anchor system of claim 21, wherein the hinged portion includes a first hinged portion at a first end of the bore and a second hinged portion at a second end of the bore.
 24. The suture anchor system of claim 20, wherein the suture receiving portion includes a first eyelet and a second eyelet positioned substantially perpendicular and spaced apart from the first eyelet.
 25. The suture anchor system of claim 20, wherein the suture receiving portion includes a C-shaped opening defined by the insert having a necked portion. 